2-(4-Chlorophenyl)-1,3-dithiane is an organic compound characterized by its unique structure, which includes a dithiane ring and a para-chlorophenyl substituent. The presence of the dithiane moiety contributes to its reactivity, particularly in nucleophilic substitution reactions, making it a valuable intermediate in organic synthesis. The chlorophenyl group enhances its lipophilicity and may influence its biological activity. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and specific conditions. It is soluble in organic solvents, which facilitates its use in various chemical reactions. The compound's stability is generally good under standard conditions, although it may be sensitive to strong oxidizing agents. Safety precautions should be taken when handling this substance, as it may pose health risks, including irritation to the skin and eyes. Overall, 2-(4-Chlorophenyl)-1,3-dithiane serves as an important building block in the synthesis of more complex organic molecules.

2-(4-Chlorophenyl)-1,3-dithiane

10359-09-8: , m-Dithiane, 2-(p-chlorophenyl)-, 1,3-Dithiane, 2-(4-chlorophenyl)-, Benzaldehyde, p-chloro-, cyclic trimethylene mercaptole, 2-(4-Chlorophenyl)-1,3-dithiane, , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 

1,3-Dithiane, 2-(4-chlorophenyl)-

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CAS 10359-09-8: 2-(4-Chlorophenyl)-1,3-dithiane

1,3-Dithiane, 2-(4-chlorophenyl)-

Ref: IN-DA01OSE4

2-(4-Chlorophenyl)-1,3-dithiane

Ref: 3D-KAA35909

2-(4-Chlorophenyl)-1,3-dithiane

Ref: 3B-C3649